Orofaciodigital Syndrome Vii; Ofd7

Description

Facial asymmetry, pseudocleft lip, lobulated tongue, hydronephrosis, delayed development, and low intelligence.

Clinical Features

Top most frequent phenotypes and symptoms related to Orofaciodigital Syndrome Vii; Ofd7

  • Hypertelorism
  • Clinodactyly
  • Hydronephrosis
  • Cleft lip
  • Abnormality of the kidney
  • Facial asymmetry
  • Preauricular skin tag
  • Coarse hair
  • Polycystic kidney dysplasia
  • Abnormality of digit

And another 3 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Orofaciodigital Syndrome Vii; Ofd7 Is also known as ofds vii, whelan syndrome, oral-facial-digital syndrome, type vii.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Sources and references

You can check the following sources for additional information.

OMIM ORPHANET MESH Genetic Syndrome Finder

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